Snore Stop Oralspray
NDC Package 61152-601-59
Package Information
Snore Stop Oralspray (atropa belladonna, ephedra distachya flowering twig, histamine, goldenseal, potassium dichromate, strychnos nux vomica seed, teucrium marum) sprays is adults and children 12 years of age and older: Spray twice under the tongue and twice at the back of the throat at bedtime.Use 30 minutes apart from any food, water or medicine.Initially, depress pump until primed.Please allow 3-5 days for initial treatmentConsult a physician for use in children under 12 years of age.Use additionally as needed, up to 4 times per day.Storage: Store upright in a cool, dry place and away from direct sunlight. This formulation utilizes a spray delivery system. Marketed by Green Pharmaceuticals, this product is identified by NDC 61152-601.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 61152 - Green Pharmaceuticals
- 61152-601 - Snore Stop Oralspray
- 61152-601-59 - 59 mL in 1 BOTTLE, SPRAY
- 61152-601 - Snore Stop Oralspray
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 61152-601-59 identifies a specific commercial package of 59 ml in 1 bottle, spray of Snore Stop Oralspray, a human over the counter drug labeled by Green Pharmaceuticals. This spray is formulated for oral use and contains strychnos nux-vomica seed; histamine; potassium dichromate; goldenseal; atropa belladonna; teucrium marum; ephedra distachya flowering twig as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Green Pharmaceuticals on April 01, 2026. The current certification is valid through December 31, 2027.
How is this Green Pharmaceuticals product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 61152060159. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.